Biology:Chromosome 19
Chromosome 19 | |
---|---|
Human chromosome 19 pair after G-banding. One is from mother, one is from father. | |
Chromosome 19 pair in human male karyogram. | |
Features | |
Length (bp) | 61,707,364 bp (CHM13) |
No. of genes | 1,357 (CCDS)[1] |
Type | Autosome |
Centromere position | Metacentric[2] (26.2 Mbp[3]) |
Complete gene lists | |
CCDS | Gene list |
HGNC | Gene list |
UniProt | Gene list |
NCBI | Gene list |
External map viewers | |
Ensembl | Chromosome 19 |
Entrez | Chromosome 19 |
NCBI | Chromosome 19 |
UCSC | Chromosome 19 |
Full DNA sequences | |
RefSeq | NC_000019 (FASTA) |
GenBank | CM000681 (FASTA) |
Chromosome 19 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 19 spans more than 61.7 million base pairs, the building material of DNA. It is considered the most gene-rich chromosome containing roughly 1,500 genes, despite accounting for only 2 percent of the human genome.[4][5]
Genes
Number of genes
The following are some of the gene count estimates of human chromosome 19. Because researchers use different approaches to genome annotation, their predictions of the number of genes on each chromosome varies (for technical details, see gene prediction). Among various projects, the collaborative consensus coding sequence project (CCDS) takes an extremely conservative strategy. So CCDS's gene number prediction represents a lower bound on the total number of human protein-coding genes.[6]
Estimated by | Protein-coding genes | Non-coding RNA genes | Pseudogenes | Source | Release date |
---|---|---|---|---|---|
CCDS | 1,357 | — | — | [1] | 2016-09-08 |
HGNC | 1,372 | 299 | 413 | [7] | 2017-05-12 |
Ensembl | 1,469 | 894 | 514 | [8] | 2017-03-29 |
UniProt | 1,435 | — | — | [9] | 2018-02-28 |
NCBI | 1,430 | 604 | 528 | [10][11][12] | 2017-05-19 |
Gene list
The following is a partial list of genes on human chromosome 19. For complete list, see the link in the infobox on the right.
Short arm
Long arm
Diseases and disorders
The following diseases are some of those related to genes on chromosome 19:[15]
- Alternating hemiplegia of childhood
- Alzheimer's disease
- CADASIL
- Centronuclear myopathy autosomal dominant form
- Charcot–Marie–Tooth disease
- Congenital hearing loss
- Congenital hypothyroidism
- Donohue syndrome
- Familial hemiplegic migraine
- Glutaric acidemia type 1
- Hemochromatosis
- HUPRA syndrome[16]
- Leber congenital amaurosis[17]
- Maple syrup urine disease
- Multiple epiphyseal dysplasia
- Myotonic dystrophy
- Myotubular myopathy autosomal dominant form
- Oligodendroglioma
- Peutz–Jeghers syndrome
- Prolidase deficiency
- Pseudoachondroplasia
- Spinocerebellar ataxia type 6
- X-linked agammaglobulinemia or Bruton's disease
Cytogenetic band
Chr. | Arm[23] | Band[24] | ISCN start[25] |
ISCN stop[25] |
Basepair start |
Basepair stop |
Stain[26] | Density |
---|---|---|---|---|---|---|---|---|
19 | p | 13.3 | 0 | 578 | 1 | 6,900,000 | gneg | |
19 | p | 13.2 | 578 | 870 | 6,900,001 | 12,600,000 | gpos | 25 |
19 | p | 13.13 | 870 | 1034 | 12,600,001 | 13,800,000 | gneg | |
19 | p | 13.12 | 1034 | 1216 | 13,800,001 | 16,100,000 | gpos | 25 |
19 | p | 13.11 | 1216 | 1581 | 16,100,001 | 19,900,000 | gneg | |
19 | p | 12 | 1581 | 1809 | 19,900,001 | 24,200,000 | gvar | |
19 | p | 11 | 1809 | 1992 | 24,200,001 | 26,200,000 | acen | |
19 | q | 11 | 1992 | 2159 | 26,200,001 | 28,100,000 | acen | |
19 | q | 12 | 2159 | 2372 | 28,100,001 | 31,900,000 | gvar | |
19 | q | 13.11 | 2372 | 2569 | 31,900,001 | 35,100,000 | gneg | |
19 | q | 13.12 | 2569 | 2737 | 35,100,001 | 37,800,000 | gpos | 25 |
19 | q | 13.13 | 2737 | 2949 | 37,800,001 | 38,200,000 | gneg | |
19 | q | 13.2 | 2949 | 3101 | 38,200,001 | 42,900,000 | gpos | 25 |
19 | q | 13.31 | 3101 | 3193 | 42,900,001 | 44,700,000 | gneg | |
19 | q | 13.32 | 3193 | 3390 | 44,700,001 | 47,500,000 | gpos | 25 |
19 | q | 13.33 | 3390 | 3649 | 47,500,001 | 50,900,000 | gneg | |
19 | q | 13.41 | 3649 | 3770 | 50,900,001 | 53,100,000 | gpos | 25 |
19 | q | 13.42 | 3770 | 3938 | 53,100,001 | 55,800,000 | gneg | |
19 | q | 13.43 | 3938 | 4120 | 55,800,001 | 58,617,616 | gpos | 25 |
References
- ↑ 1.0 1.1 "Search results - 19[CHR] AND "Homo sapiens"[Organism] AND ("has ccds"[Properties] AND alive[prop]) - Gene". 2016-09-08. https://www.ncbi.nlm.nih.gov/gene?term=19%5BChr%5D%20AND%20%22Homo%20sapiens%22%5BOrganism%5D%20AND%20%28%22has%20ccds%22%5BProperties%5D%20AND%20alive%5Bprop%5D%29&cmd=DetailsSearch.
- ↑ Tom Strachan; Andrew Read (2 April 2010). Human Molecular Genetics. Garland Science. p. 45. ISBN 978-1-136-84407-2. https://books.google.com/books?id=dSwWBAAAQBAJ&pg=PA45.
- ↑ 3.0 3.1 Genome Decoration Page, NCBI. Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3). Last update 2014-06-03. Retrieved 2017-04-26.
- ↑ Ucciferri, Charles (2004-03-31). "Gene-Rich Human Chromosome 19 Sequence Completed" (in en-US). https://jgi.doe.gov/news_3_31_04/.
- ↑ Sehgal, N.; Fritz, A. J.; Morris, K.; Torres, I.; Chen, Z.; Xu, J.; Berezney, R. (2014). "Gene Density and Chromosome Territory Shape". Chromosoma 123 (5): 499–513. doi:10.1007/s00412-014-0480-y. PMID 25106753.
- ↑ Pertea M, Salzberg SL (2010). "Between a chicken and a grape: estimating the number of human genes.". Genome Biol 11 (5): 206. doi:10.1186/gb-2010-11-5-206. PMID 20441615.
- ↑ "Statistics & Downloads for chromosome 19". 2017-05-12. https://www.genenames.org/cgi-bin/statistics?c=19.
- ↑ "Chromosome 19: Chromosome summary - Homo sapiens". 2017-03-29. http://mar2017.archive.ensembl.org/Homo_sapiens/Location/Chromosome?r=19.
- ↑ "Human chromosome 19: entries, gene names and cross-references to MIM". 2018-02-28. https://www.uniprot.org/docs/humchr19.txt.
- ↑ "Search results - 19[CHR] AND "Homo sapiens"[Organism] AND ("genetype protein coding"[Properties] AND alive[prop]) - Gene". 2017-05-19. https://www.ncbi.nlm.nih.gov/gene?term=19%5BCHR%5D%20AND%20%22Homo%20sapiens%22%5BOrganism%5D%20AND%20%28%22genetype%20protein%20coding%22%5BProperties%5D%20AND%20alive%5Bprop%5D%29&cmd=DetailsSearch.
- ↑ "Search results - 19[CHR] AND "Homo sapiens"[Organism] AND ( ("genetype miscrna"[Properties] OR "genetype ncrna"[Properties] OR "genetype rrna"[Properties] OR "genetype trna"[Properties] OR "genetype scrna"[Properties] OR "genetype snrna"[Properties] OR "genetype snorna"[Properties]) NOT "genetype protein coding"[Properties] AND alive[prop]) - Gene". 2017-05-19. https://www.ncbi.nlm.nih.gov/gene?term=19%5BCHR%5D%20AND%20%22Homo%20sapiens%22%5BOrganism%5D%20AND%20%28%28%22genetype%20miscrna%22%5BProperties%5D%20OR%20%22genetype%20ncrna%22%5BProperties%5D%20OR%20%22genetype%20rrna%22%5BProperties%5D%20OR%20%22genetype%20trna%22%5BProperties%5D%20OR%20%22genetype%20scrna%22%5BProperties%5D%20OR%20%22genetype%20snrna%22%5BProperties%5D%20OR%20%22genetype%20snorna%22%5BProperties%5D%29%20NOT%20%22genetype%20protein%20coding%22%5BProperties%5D%20AND%20alive%5Bprop%5D%29&cmd=DetailsSearch.
- ↑ "Search results - 19[CHR] AND "Homo sapiens"[Organism] AND ("genetype pseudo"[Properties] AND alive[prop]) - Gene". 2017-05-19. https://www.ncbi.nlm.nih.gov/gene?term=19%5BCHR%5D%20AND%20%22Homo%20sapiens%22%5BOrganism%5D%20AND%20%28%22genetype%20pseudo%22%5BProperties%5D%20AND%20alive%5Bprop%5D%29&cmd=DetailsSearch.
- ↑ "2E4/Kaptin (KPTN)—a candidate gene for the hearing loss locus, DFNA4". Ann Hum Genet 64 (3): 189–196. 2000. doi:10.1046/j.1469-1809.2000.6430189.x. PMID 11409409.
- ↑ 14.0 14.1 Dean, L. (2005). "Ch. 5: The ABO blood group". Blood Groups and Red Cell Antigens. Bethesda MD: National Center for Biotechnology Information. NBK2261. https://www.ncbi.nlm.nih.gov/books/NBK2267/.
- ↑ Gilbert F (1997). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 19". Genet Test 1 (2): 145–9. doi:10.1089/gte.1997.1.145. PMID 10464639.
- ↑ "OMIM Entry - # 613845 - HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME; HUPRAS" (in en-us). https://www.omim.org/entry/613845.
- ↑ Moss, K (Spring 2001). "Leber's Congenital Amaurosis". Texas Deafblind Outreach. Texas School for the Blind and Visually Impaired. http://www.tsbvi.edu/seehear/spring01/lebers.htm.
- ↑ Genome Decoration Page, NCBI. Ideogram data for Homo sapience (400 bphs, Assembly GRCh38.p3). Last update 2014-03-04. Retrieved 2017-04-26.
- ↑ Genome Decoration Page, NCBI. Ideogram data for Homo sapience (550 bphs, Assembly GRCh38.p3). Last update 2015-08-11. Retrieved 2017-04-26.
- ↑ International Standing Committee on Human Cytogenetic Nomenclature (2013). ISCN 2013: An International System for Human Cytogenetic Nomenclature (2013). Karger Medical and Scientific Publishers. ISBN 978-3-318-02253-7. https://books.google.com/books?id=lGCLrh0DIwEC.
- ↑ Sethakulvichai, W.; Manitpornsut, S.; Wiboonrat, M.; Lilakiatsakun, W.; Assawamakin, A.; Tongsima, S. (2012). "Estimation of band level resolutions of human chromosome images". 2012 Ninth International Conference on Computer Science and Software Engineering (JCSSE). pp. 276–282. doi:10.1109/JCSSE.2012.6261965. ISBN 978-1-4673-1921-8. https://www.researchgate.net/publication/261304470.
- ↑ Genome Decoration Page, NCBI. Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3). Last update 2014-06-03. Retrieved 2017-04-26.
- ↑ "p": Short arm; "q": Long arm.
- ↑ For cytogenetic banding nomenclature, see article locus.
- ↑ 25.0 25.1 These values (ISCN start/stop) are based on the length of bands/ideograms from the ISCN book, An International System for Human Cytogenetic Nomenclature (2013). Arbitrary unit.
- ↑ gpos: Region which is positively stained by G banding, generally AT-rich and gene poor; gneg: Region which is negatively stained by G banding, generally CG-rich and gene rich; acen Centromere. var: Variable region; stalk: Stalk.
- "The DNA sequence and biology of human chromosome 19". Nature 428 (6982): 529–35. 2004. doi:10.1038/nature02399. PMID 15057824. Bibcode: 2004Natur.428..529G.
- Human Proteome Project Launch website~ https://web.archive.org/web/20110726163128/http://www.hupo.org/research/hpp/HPP_legrain_sep_2010.pdf
External links
- National Institutes of Health. "Chromosome 19". Genetics Home Reference. http://ghr.nlm.nih.gov/chromosome=19.
- "Chromosome 19". http://web.ornl.gov/sci/techresources/Human_Genome/posters/chromosome/chromo19.shtml.
Original source: https://en.wikipedia.org/wiki/Chromosome 19.
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